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ORDER NO. 03502 ENTERED AUG 21 2003 This is an electronic copy. Format and font may vary from the official version. Attachments may not appear. BEFORE THE PUBLIC UTILITY COMMISSION OF OREGON UM 1095
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Identify the research question that the randomized controlled clinical trial will address.
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Design the study protocol including the eligibility criteria for participants, randomization process, intervention details, and outcome measures.
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Obtain necessary approvals from ethics committees and regulatory bodies.
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Recruit participants who meet the eligibility criteria and obtain informed consent.
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Randomly assign participants to either the intervention group or the control group.
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Implement the intervention according to the study protocol.
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Monitor and collect data on the outcomes of interest.
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Analyze the data using appropriate statistical methods.
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Interpret the results and draw conclusions based on the findings.

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A randomized controlled clinical trial is a type of scientific experiment designed to assess the efficacy of a new treatment or intervention by randomly assigning patients to different groups.
Researchers, pharmaceutical companies, or other entities conducting clinical trials are required to file a randomized controlled clinical.
To fill out a randomized controlled clinical, researchers must follow strict protocols outlined in the trial design, including random assignment of participants and collecting data on outcomes.
The purpose of a randomized controlled clinical trial is to provide reliable evidence on the effectiveness of a new treatment or intervention by minimizing bias and confounding factors.
A randomized controlled clinical trial must report details of the study design, participant characteristics, intervention protocols, outcomes measured, and statistical analysis methods.
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